PubMed:21903317 / 1093-1176 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T8","span":{"begin":0,"end":83},"obj":"Sentence"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-entities","denotations":[{"id":"8882","span":{"begin":32,"end":35},"obj":"GeneOrGeneProduct"},{"id":"8883","span":{"begin":65,"end":73},"obj":"OrganismTaxon"},{"id":"8884","span":{"begin":79,"end":82},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A32","pred":"db_id","subj":"8882","obj":"NCBIGene:5972"},{"id":"A33","pred":"db_id","subj":"8883","obj":"NCBITaxon:9606"},{"id":"A34","pred":"db_id","subj":"8884","obj":"MESH:D051436"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T7","span":{"begin":50,"end":54},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0021136"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T32","span":{"begin":8,"end":13},"obj":"GeneOrGeneProduct"},{"id":"T33","span":{"begin":32,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T34","span":{"begin":36,"end":45},"obj":"GeneOrGeneProduct"},{"id":"T35","span":{"begin":50,"end":54},"obj":"GeneOrGeneProduct"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T22","span":{"begin":32,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":50,"end":54},"obj":"GeneOrGeneProduct"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T13","span":{"begin":79,"end":82},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A13","pred":"originalLabel","subj":"T13","obj":"D051436"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T14","span":{"begin":32,"end":35},"obj":"GeneOrGeneProduct"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T10","span":{"begin":79,"end":82},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A10","pred":"mondo_id","subj":"T10","obj":"0005300"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T15","span":{"begin":79,"end":82},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A15","pred":"ID:","subj":"T15","obj":"D051436"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T14","span":{"begin":79,"end":82},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A14","pred":"#label","subj":"T14","obj":"D051436"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":65,"end":73},"obj":"OrganismTaxon"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T20","span":{"begin":32,"end":35},"obj":"ChemicalEntity"}],"attributes":[{"id":"A20","pred":"ID:","subj":"T20","obj":"D012083"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T20","span":{"begin":32,"end":35},"obj":"ChemicalEntity"},{"id":"T14","span":{"begin":32,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T28823","span":{"begin":79,"end":82},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T28669","span":{"begin":65,"end":73},"obj":"OrganismTaxon"}],"attributes":[{"id":"A20","pred":"ID:","subj":"T20","obj":"D012083"},{"id":"A10109","pred":"#label","subj":"T28823","obj":"D051436"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T8","span":{"begin":0,"end":83},"obj":"Sentence"},{"id":"T8","span":{"begin":0,"end":83},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"On this basis, we conclude that REN mutations are rare events in patients with CKD."}